Sb bicolor PI562621 PH538 (pi562621ph538) ▼
Most severe consequence
 
missense variant
Alleles
A/G
Location

Chromosome 2:167163 (forward strand)|VCF:2  167163  rs5417869278  A  G

HGVS names

This variant has 3 HGVS names - Show

External Links

Original source

EVA2024_rsID_mapped

About this variant

This variant overlaps 4 transcripts.